Modeling linkage disequilibrium in exact linkage computations: a comparison of first-order Markov approaches and the clustered-markers approach

por Albers, Cornelis A, Kappen, Hilbert J
Publicado 2007

The Cluster Variation Method for Efficient Linkage Analysis on Extended Pedigrees

por Albers, Cornelis A, Leisink, Martijn AR, Kappen, Hilbert J
Publicado 2006

Investigating the effect of dependence between conditions with Bayesian Linear Mixed Models for motif activity analysis

por Lederer, Simone, Heskes, Tom, van Heeringen, Simon J., Albers, Cornelis A.
Publicado 2020

ONECUT transcription factors induce neuronal characteristics and remodel chromatin accessibility

por van der Raadt, Jori, van Gestel, Sebastianus H C, Nadif Kasri, Nael, Albers, Cornelis A
Publicado 2019

Quantification of differential gene expression by multiplexed targeted resequencing of cDNA

por Arts, Peer, van der Raadt, Jori, van Gestel, Sebastianus H.C., Steehouwer, Marloes, Shendure, Jay, Hoischen, Alexander, Albers, Cornelis A.
Publicado 2017

Bayesian neural networks with variable selection for prediction of genotypic values

por van Bergen, Giel H. H., Duenk, Pascal, Albers, Cornelis A., Bijma, Piter, Calus, Mario P. L., Wientjes, Yvonne C. J., Kappen, Hilbert J.
Publicado 2020

Maps of open chromatin highlight cell type–restricted patterns of regulatory sequence variation at hematological trait loci

por Paul, Dirk S., Albers, Cornelis A., Rendon, Augusto, Voss, Katrin, Stephens, Jonathan, van der Harst, Pim, Chambers, John C., Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Publicado 2013

Rapid Neuronal Differentiation of Induced Pluripotent Stem Cells for Measuring Network Activity on Micro-electrode Arrays

por Frega, Monica, van Gestel, Sebastianus H. C., Linda, Katrin, van der Raadt, Jori, Keller, Jason, Van Rhijn, Jon-Ruben, Schubert, Dirk, Albers, Cornelis A., Nadif Kasri, Nael
Publicado 2017

The variant call format and VCFtools

por Danecek, Petr, Auton, Adam, Abecasis, Goncalo, Albers, Cornelis A., Banks, Eric, DePristo, Mark A., Handsaker, Robert E., Lunter, Gerton, Marth, Gabor T., Sherry, Stephen T., McVean, Gilean, Durbin, Richard
Publicado 2011

Immuno-detection by sequencing enables large-scale high-dimensional phenotyping in cells

por van Buggenum, Jessie A. G., Gerlach, Jan P., Tanis, Sabine E. J., Hogeweg, Mark, Jansen, Pascal W. T. C., Middelwijk, Jesse, van der Steen, Ruud, Vermeulen, Michiel, Stunnenberg, Hendrik G., Albers, Cornelis A., Mulder, Klaas W.
Publicado 2018

Dynamics of gene silencing during X inactivation using allele-specific RNA-seq

por Marks, Hendrik, Kerstens, Hindrik H. D., Barakat, Tahsin Stefan, Splinter, Erik, Dirks, René A. M., van Mierlo, Guido, Joshi, Onkar, Wang, Shuang-Yin, Babak, Tomas, Albers, Cornelis A., Kalkan, Tüzer, Smith, Austin, Jouneau, Alice, de Laat, Wouter, Gribnau, Joost, Stunnenberg, Hendrik G.
Publicado 2015

Erratum to: Dynamics of gene silencing during X inactivation using allele-specific RNA-seq

por Marks, Hendrik, Kerstens, Hindrik H. D., Barakat, Tahsin Stefan, Splinter, Erik, Dirks, René A. M., van Mierlo, Guido, Joshi, Onkar, Wang, Shuang-Yin, Babak, Tomas, Albers, Cornelis A., Kalkan, Tüzer, Smith, Austin, Jouneau, Alice, de Laat, Wouter, Gribnau, Joost, Stunnenberg, Hendrik G.
Publicado 2016

Exome sequencing identifies NBEAL2 as the causative gene for Gray Platelet Syndrome

por Albers, Cornelis A, Cvejic, Ana, Favier, Rémi, Bouwmans, Evelien E, Alessi, Marie-Christine, Bertone, Paul, Jordan, Gregory, Kettleborough, Ross NW, Kiddle, Graham, Kostadima, Myrto, Read, Randy J, Sipos, Botond, Sivapalaratnam, Suthesh, Smethurst, Peter A, Stephens, Jonathan, Voss, Katrin, Nurden, Alan, Rendon, Augusto, Nurden, Paquita, Ouwehand, Willem H
Publicado 2011

The origin, evolution, and functional impact of short insertion–deletion variants identified in 179 human genomes

por Montgomery, Stephen B., Goode, David L., Kvikstad, Erika, Albers, Cornelis A., Zhang, Zhengdong D., Mu, Xinmeng Jasmine, Ananda, Guruprasad, Howie, Bryan, Karczewski, Konrad J., Smith, Kevin S., Anaya, Vanessa, Richardson, Rhea, Davis, Joe, MacArthur, Daniel G., Sidow, Arend, Duret, Laurent, Gerstein, Mark, Makova, Kateryna D., Marchini, Jonathan, McVean, Gil, Lunter, Gerton
Publicado 2013

Inheritance of low-frequency regulatory SNPs and a rare null mutation in exon-junction complex subunit RBM8A causes TAR

por Albers, Cornelis A, Paul, Dirk S, Schulze, Harald, Freson, Kathleen, Stephens, Jonathan C, Smethurst, Peter A, Jolley, Jennifer D, Cvejic, Ana, Kostadima, Myrto, Bertone, Paul, Breuning, Martijn H, Debili, Najet, Deloukas, Panos, Favier, Rémi, Fiedler, Janine, Hobbs, Catherine M, Huang, Ni, Hurles, Matthew E, Kiddle, Graham, Krapels, Ingrid, Nurden, Paquita, Ruivenkamp, Claudia A L, Sambrook, Jennifer G, Smith, Kenneth, Stemple, Derek L, Strauss, Gabriele, Thys, Chantal, van Geet, Christel, Newbury-Ecob, Ruth, Ouwehand, Willem H, Ghevaert, Cedric
Publicado 2012

Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells

por Chen, Lu, Ge, Bing, Casale, Francesco Paolo, Vasquez, Louella, Kwan, Tony, Garrido-Martín, Diego, Watt, Stephen, Yan, Ying, Kundu, Kousik, Ecker, Simone, Datta, Avik, Richardson, David, Burden, Frances, Mead, Daniel, Mann, Alice L., Fernandez, Jose Maria, Rowlston, Sophia, Wilder, Steven P., Farrow, Samantha, Shao, Xiaojian, Lambourne, John J., Redensek, Adriana, Albers, Cornelis A., Amstislavskiy, Vyacheslav, Ashford, Sofie, Berentsen, Kim, Bomba, Lorenzo, Bourque, Guillaume, Bujold, David, Busche, Stephan, Caron, Maxime, Chen, Shu-Huang, Cheung, Warren, Delaneau, Oliver, Dermitzakis, Emmanouil T., Elding, Heather, Colgiu, Irina, Bagger, Frederik O., Flicek, Paul, Habibi, Ehsan, Iotchkova, Valentina, Janssen-Megens, Eva, Kim, Bowon, Lehrach, Hans, Lowy, Ernesto, Mandoli, Amit, Matarese, Filomena, Maurano, Matthew T., Morris, John A., Pancaldi, Vera, Pourfarzad, Farzin, Rehnstrom, Karola, Rendon, Augusto, Risch, Thomas, Sharifi, Nilofar, Simon, Marie-Michelle, Sultan, Marc, Valencia, Alfonso, Walter, Klaudia, Wang, Shuang-Yin, Frontini, Mattia, Antonarakis, Stylianos E., Clarke, Laura, Yaspo, Marie-Laure, Beck, Stephan, Guigo, Roderic, Rico, Daniel, Martens, Joost H.A., Ouwehand, Willem H., Kuijpers, Taco W., Paul, Dirk S., Stunnenberg, Hendrik G., Stegle, Oliver, Downes, Kate, Pastinen, Tomi, Soranzo, Nicole
Publicado 2016